Cas 91473-15-3,2-(5,5,8,8-tetraphenyl-2,4,9-trioxatricyklo<5,2,0,0<sup>3,6</sup>>-3-nonyl)-1,3-dioxolane

91473-15-3

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Basic information

Product Name: 2-(5,5,8,8-tetraphenyl-2,4,9-trioxatricyklo<5,2,0,0^3,6>-3-nonyl)-1,3-dioxolane
Synonyms:
CAS NO:91473-15-3
Molecular Formula:
Molecular Weight: 504.582
EINECS: N/A
Product Categories: N/A
Mol File: 91473-15-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(5,5,8,8-tetraphenyl-2,4,9-trioxatricyklo<5,2,0,0^3,6>-3-nonyl)-1,3-dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-(5,5,8,8-tetraphenyl-2,4,9-trioxatricyklo<5,2,0,0^3,6>-3-nonyl)-1,3-dioxolane(91473-15-3)
EPA Substance Registry System: 2-(5,5,8,8-tetraphenyl-2,4,9-trioxatricyklo<5,2,0,0^3,6>-3-nonyl)-1,3-dioxolane(91473-15-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 91473-15-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91473-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91473-15:
(7*9)+(6*1)+(5*4)+(4*7)+(3*3)+(2*1)+(1*5)=133
133 % 10 = 3
So 91473-15-3 is a valid CAS Registry Number.

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91473-15-3Relevant articles and documents

PHOTOCHEMICAL REACTIONS OF 2-SUBSTITUTED FURANS WITH SOME CARBONYL COMPOUNDS

Sekretar, Stanislav,Ruda, Jana,Stibranyi, Ladislav

, p. 71 - 77 (2007/10/02)

Photochemical reactions of 2-substituted furans I, IV and V with benzaldehyde, benzophenone and 4-methylbenzophenone gave substituted 2,7-dioxabicyklo-3-heptenes, which can be used for syntheses of 2,3- or 2,4-disubstituted furans.Regioisomeric (2:1)-cycloadducts XV and XVI were distinguished on the basis of their 1H and 13C NMR spectra.

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